Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 44
Filter
Add more filters










Publication year range
2.
Article in English | MEDLINE | ID: mdl-35449718

ABSTRACT

Significant sensitivity improvements have been achieved by utilizing high temperature superconducting (HTS) resonators in nuclear magnetic resonance (NMR) probes. Many nuclei such as 13C benefit from strong excitation fields which cannot be produced by traditional HTS resonator designs. We investigate the use of double-sided, counter-wound multi-arm spiral HTS resonators with the aim of increasing the excitation field at the required nuclear Larmor frequency for 13C. When compared to double-sided, counter-wound spiral resonators with similar geometry, simulations indicate that the multi-arm spiral version develops a more uniform current distribution. Preliminary tests of a two-arm resonator indicate that it may produce a stronger excitation field.

3.
Article in English | MEDLINE | ID: mdl-33867781

ABSTRACT

Nuclear magnetic resonance (NMR) probes using thin-film high temperature superconducting (HTS) resonators offer high sensitivity and are particularly suitable for small-sample applications. We are developing an improved 1.5 mm HTS NMR probe designed for operation at 14.1 T and optimized for 13C detection. The total sample volume is about 35 µL and the active sample volume is 20 µL. The probe employs HTS resonators for 13C and 1H transmission and detection and the 2H lock. We examine the interactions of multiple superconducting resonators and normal metal tuning loops on coil resonance frequency and probe sensitivity. We test a recently introduced 13C resonator design, engineered to significantly increase 13C detection sensitivity over previous all-HTS probes. At zero field, we observe a 13C quality factor of 6000 which is several times higher than previous resonators. In this work the coil design considerations and probe build-out procedure are discussed.

4.
Proc IEEE Conf Decis Control ; 2021: 611-616, 2021 Dec.
Article in English | MEDLINE | ID: mdl-38420271

ABSTRACT

High magnetic fields significantly improve the resolution and sensitivity of nuclear magnetic resonance (NMR) spectroscopy measurements, which presents exciting research opportunities in areas of chemistry, biology, and material science. Powered magnets can provide much higher magnetic fields than persistent mode superconducting magnets but suffer from temporal magnetic field fluctuations due to power supply ripple and variations in cooling water temperature and flow rate which make powered magnets non-viable for high resolution NMR experiments. Previous work has demonstrated that a multi-rate sampled data cascade control system may be used to improve the resolution of NMR experiments in powered magnets. Despite these advances in reducing temporal magnetic field fluctuations, the field regulation design does not accommodate the use of pulsed field gradients, which are necessary in many NMR experiments. This work presents a control topology which accommodates the use of pulsed field gradient signals with the field regulation system. This control approach is verified using NMR measurements.

5.
Article in English | MEDLINE | ID: mdl-31857782

ABSTRACT

Replacing normal metal NMR coils with thin-film high-temperature superconductor (HTS) resonators can significantly improve the sensitivity of analytical NMR. To study the use of these resonators for excitation as well as detection, we investigated the radio frequency properties of the HTS NMR coils in both frequency and time domain at a variety of transmit power levels. Experiments were conducted on a double-sided, counter wound spiral resonator designed to detect NMR signals from 13C nuclei at 14.1 T. Power-dependent nonlinearity was observed in the transmission coefficient and quality factor. The ability of the HTS resonators to accurately generate short pulses was studied in the time domain over the range power levels. The results of this study show that some form of Q switching is needed to get good transmit performance from HTS coils for 13C. For that purpose, the effect of adding a shorted transmission line stub to improve the pulse shapes and reduce phase transients was studied.

6.
J Magn Reson ; 301: 109-118, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30870670

ABSTRACT

Powered resistive and resistive-superconductive hybrid magnets can reach fields higher than superconducting NMR magnets but lack the field homogeneity and temporal stability needed for high resolution NMR. Due to field fluctuations in powered magnets, commercially available mapping systems fail to produce maps of these magnets with sufficient reproducibility, thus hampering attempts to improve homogeneity of the field they generate. Starting with a commercial mapper, we built a mapping system which uses a two-channel (measurement + reference) mapper probe. We used this system to map and then to shim two magnets of Florida Bitter type at the National High Magnetic Field Laboratory in Tallahassee, FL. With a combination of passive (ferromagnetic) and active shims we achieved 2.3 ppm homogeneity in 1 cm diameter spherical volume (dsv) at 25.0 T in the Keck resistive magnet, and 0.9 ppm homogeneity in 1 cm dsv at 23.5, 28.2, and 35.2 T in the series-connected resistive-superconductive hybrid (SCH) magnet.

7.
J Magn Reson ; 289: 35-44, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29459343

ABSTRACT

Nuclear magnetic resonance (NMR) is an intrinsically insensitive technique, with Boltzmann distributions of nuclear spin states on the order of parts per million in conventional magnetic fields. To overcome this limitation, dynamic nuclear polarization (DNP) can be used to gain up to three orders of magnitude in signal enhancement, which can decrease experimental time by up to six orders of magnitude. In DNP experiments, nuclear spin polarization is enhanced by transferring the relatively larger electron polarization to NMR active nuclei via microwave irradiation. Here, we describe the design and performance of a quasi-optical system enabling the use of a single 395 GHz gyrotron microwave source to simultaneously perform DNP experiments on two different 14.1 T (1H 600 MHz) NMR spectrometers: one configured for magic angle spinning (MAS) solid state NMR; the other configured for solution state NMR experiments. In particular, we describe how the high power microwave beam is split, transmitted, and manipulated between the two spectrometers. A 13C enhancement of 128 is achieved via the cross effect for alanine, using the nitroxide biradical AMUPol, under MAS-DNP conditions at 110 K, while a 31P enhancement of 160 is achieved via the Overhauser effect for triphenylphosphine using the monoradical BDPA under solution NMR conditions at room temperature. The latter result is the first demonstration of Overhauser DNP in the solution state at a field of 14.1 T (1H 600 MHz). Moreover these results have been produced with large sample volumes (∼100 µL, i.e. 3 mm diameter NMR tubes).

8.
Article in English | MEDLINE | ID: mdl-29038639

ABSTRACT

Nuclear Magnetic Resonance (NMR) probes based on High Temperature Superconducting (HTS) resonators have demonstrated significant gains in detection sensitivity. However, the widespread acceptance of this technology has been limited by some unresolved issues including the mechanical unreliability of the moveable inductive loops used to adjust tuning and matching. In order to improve reliability, we propose to implement frequency tuning and impedance matching of HTS resonators using fixed inductively coupled loops and variable capacitors. By analyzing the loss mechanisms associated with inductive loops, we predict that using a superconducting inductive loop for tuning and matching will not only improve the reliability of HTS probes, but also provide improvements in sensitivity.

9.
J Magn Reson ; 284: 125-136, 2017 11.
Article in English | MEDLINE | ID: mdl-28890288

ABSTRACT

The National High Magnetic Field Laboratory has brought to field a Series-Connected Hybrid magnet for NMR spectroscopy. As a DC powered magnet it can be operated at fields up to 36.1T. The series connection between a superconducting outsert and a resistive insert dramatically minimizes the high frequency fluctuations of the magnetic field typically observed in purely resistive magnets. Current-density-grading among various resistive coils was used for improved field homogeneity. The 48mm magnet bore and 42mm outer diameter of the probes leaves limited space for conventional shims and consequently a combination of resistive and ferromagnetic shims are used. Field maps corrected for field instabilities were obtained and shimming achieved better than 1ppm homogeneity over a cylindrical volume of 1cm diameter and height. The magnetic field is regulated within 0.2ppm using an external 7Li lock sample doped with paramagnetic MnCl2. The improved field homogeneity and field regulation using a modified AVANCE NEO console enables NMR spectroscopy at 1H frequencies of 1.0, 1.2 and 1.5GHz. NMR at 1.5GHz reflects a 50% increase in field strength above the highest superconducting magnets currently available. Three NMR probes have been constructed each equipped with an external lock rf coil for field regulation. Initial NMR results obtained from the SCH magnet using these probes illustrate the very exciting potential of ultra-high magnetic fields.


Subject(s)
Magnetic Resonance Spectroscopy/instrumentation , Magnets , Chlorides , Electromagnetic Fields , Equipment Design , Isotopes , Lithium , Manganese Compounds , Superconductivity
10.
Article in English | MEDLINE | ID: mdl-27840565

ABSTRACT

Superconducting self-resonant spiral structures are of current interest for applications both in metamaterials and as probe coils for nuclear magnetic resonance (NMR) spectroscopy for high-sensitivity chemical analysis. Accurate spiral models are available in the literature for behavior of a spiral below and up to self-resonance. However, knowledge of the higher modes is also important. We present the relationships between the spiral parameters and the multiple mode frequencies of single sided spirals on dielectric substrates as modeled by method of moments simulation. In the absence of a ground plane, we find that the mode frequency has a linear though not necessarily harmonic dependence on the mode number. The effect of a thick substrate can be approximated by an effective dielectric constant. But when the thickness is less than 20% of the spiral trace width (router - rinner) this approximation is no longer accurate. We have developed a simple empirical formula to predict the higher modes.

11.
J Am Chem Soc ; 138(42): 14066-14075, 2016 Oct 26.
Article in English | MEDLINE | ID: mdl-27701859

ABSTRACT

HIV-1 CA capsid protein possesses intrinsic conformational flexibility, which is essential for its assembly into conical capsids and interactions with host factors. CA is dynamic in the assembled capsid, and residues in functionally important regions of the protein undergo motions spanning many decades of time scales. Chemical shift anisotropy (CSA) tensors, recorded in magic-angle-spinning NMR experiments, provide direct residue-specific probes of motions on nano- to microsecond time scales. We combined NMR, MD, and density-functional-theory calculations, to gain quantitative understanding of internal backbone dynamics in CA assemblies, and we found that the dynamically averaged 15N CSA tensors calculated by this joined protocol are in remarkable agreement with experiment. Thus, quantitative atomic-level understanding of the relationships between CSA tensors, local backbone structure, and motions in CA assemblies is achieved, demonstrating the power of integrating NMR experimental data and theory for characterizing atomic-resolution dynamics in biological systems.

12.
NMR Biomed ; 29(6): 759-66, 2016 06.
Article in English | MEDLINE | ID: mdl-27061712

ABSTRACT

At ultrahigh magnetic field strengths (B0 ≥ 7.0 T), potassium ((39) K) MRI might evolve into an interesting tool for biomedical research. However, (39) K MRI is still challenging because of the low NMR sensitivity and short relaxation times. In this work, we demonstrated the feasibility of (39) K MRI at 21.1 T, determined in vivo relaxation times of the rat head at 21.1 T, and compared (39) K and sodium ((23) Na) relaxation times of model solutions containing different agarose gel concentrations at 7.0 and 21.1 T. (39) K relaxation times were markedly shorter than those of (23) Na. Compared with the lower field strength, (39) K relaxation times were up to 1.9- (T1 ), 1.4- (T2S ) and 1.9-fold (T2L ) longer at 21.1 T. The increase in the (23) Na relaxation times was less pronounced (up to 1.2-fold). Mono-exponential fits of the (39) K longitudinal relaxation time at 21.1 T revealed T1 = 14.2 ± 0.1 ms for the healthy rat head. The (39) K transverse relaxation times were 1.8 ± 0.2 ms and 14.3 ± 0.3 ms for the short (T2S ) and long (T2L ) components, respectively. (23) Na relaxation times were markedly longer (T1 = 41.6 ± 0.4 ms; T2S = 4.9 ± 0.2 ms; T2L = 33.2 ± 0.2 ms). (39) K MRI of the healthy rat head could be performed with a nominal spatial resolution of 1 × 1 × 1 mm(3) within an acquisition time of 75 min. The increase in the relaxation times with magnetic field strength is beneficial for (23) Na and (39) K MRI at ultrahigh magnetic field strength. Our results demonstrate that (39) K MRI at 21.1 T enables acceptable image quality for preclinical research. Copyright © 2016 John Wiley & Sons, Ltd.


Subject(s)
Brain/diagnostic imaging , Brain/metabolism , Magnetic Resonance Imaging/methods , Molecular Imaging/methods , Potassium/pharmacokinetics , Sodium Isotopes/pharmacokinetics , Animals , Feasibility Studies , Radiopharmaceuticals/pharmacokinetics , Rats , Rats, Inbred F344 , Reproducibility of Results , Sensitivity and Specificity , Tissue Distribution
13.
IEEE Trans Microw Theory Tech ; 63(7): 2107-2114, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26556910

ABSTRACT

This work presents an empirical formula to accurately determine the frequencies of the fundamental and higher order resonances of an Archimedean spiral in a uniform dielectric medium in the absence of a ground plane. The formula is based on method-of-moments simulations which have been experimentally validated. This empirical formula is widely applicable to a broad range of spirals from thin-ring to disk-shaped (ratio of inner to outer radii 0 to 1), with 10 or more turns.

14.
Proc Natl Acad Sci U S A ; 112(47): 14617-22, 2015 Nov 24.
Article in English | MEDLINE | ID: mdl-26553990

ABSTRACT

Host factor protein Cyclophilin A (CypA) regulates HIV-1 viral infectivity through direct interactions with the viral capsid, by an unknown mechanism. CypA can either promote or inhibit viral infection, depending on host cell type and HIV-1 capsid (CA) protein sequence. We have examined the role of conformational dynamics on the nanosecond to millisecond timescale in HIV-1 CA assemblies in the escape from CypA dependence, by magic-angle spinning (MAS) NMR and molecular dynamics (MD). Through the analysis of backbone (1)H-(15)N and (1)H-(13)C dipolar tensors and peak intensities from 3D MAS NMR spectra of wild-type and the A92E and G94D CypA escape mutants, we demonstrate that assembled CA is dynamic, particularly in loop regions. The CypA loop in assembled wild-type CA from two strains exhibits unprecedented mobility on the nanosecond to microsecond timescales, and the experimental NMR dipolar order parameters are in quantitative agreement with those calculated from MD trajectories. Remarkably, the CypA loop dynamics of wild-type CA HXB2 assembly is significantly attenuated upon CypA binding, and the dynamics profiles of the A92E and G94D CypA escape mutants closely resemble that of wild-type CA assembly in complex with CypA. These results suggest that CypA loop dynamics is a determining factor in HIV-1's escape from CypA dependence.


Subject(s)
Capsid/chemistry , Cyclophilin A/chemistry , HIV-1/chemistry , Allosteric Regulation , Capsid/ultrastructure , Cyclophilin A/ultrastructure , HIV-1/ultrastructure , Humans , Magnetic Resonance Spectroscopy , Molecular Dynamics Simulation , Mutant Proteins/chemistry , Mutation/genetics , Time Factors
15.
MAGMA ; 27(1): 63-70, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23748497

ABSTRACT

OBJECT: MR imaging of low-gamma nuclei at the ultrahigh magnetic field of 21.1 T provides a new opportunity for understanding a variety of biological processes. Among these, chlorine and sodium are attracting attention for their involvement in brain function and cancer development. MATERIALS AND METHODS: MRI of (35)Cl and (23)Na were performed and relaxation times were measured in vivo in normal rat (n = 3) and in rat with glioma (n = 3) at 21.1 T. The concentrations of both nuclei were evaluated using the center-out back-projection method. RESULTS: T 1 relaxation curve of chlorine in normal rat head was fitted by bi-exponential function (T 1a = 4.8 ms (0.7) T 1b = 24.4 ± 7 ms (0.3) and compared with sodium (T 1 = 41.4 ms). Free induction decays (FID) of chlorine and sodium in vivo were bi-exponential with similar rapidly decaying components of [Formula: see text] ms and [Formula: see text] ms, respectively. Effects of small acquisition matrix and bi-exponential FIDs were assessed for quantification of chlorine (33.2 mM) and sodium (44.4 mM) in rat brain. CONCLUSION: The study modeled a dramatic effect of the bi-exponential decay on MRI results. The revealed increased chlorine concentration in glioma (~1.5 times) relative to a normal brain correlates with the hypothesis asserting the importance of chlorine for tumor progression.


Subject(s)
Brain Neoplasms/pathology , Chlorine/chemistry , Glioma/pathology , Magnetic Resonance Imaging/methods , Sodium/chemistry , Animals , Disease Progression , Equipment Design , Imaging, Three-Dimensional , Rats
16.
J Am Chem Soc ; 135(47): 17793-803, 2013 Nov 27.
Article in English | MEDLINE | ID: mdl-24164646

ABSTRACT

A key stage in HIV-1 maturation toward an infectious virion requires sequential proteolytic cleavage of the Gag polyprotein leading to the formation of a conical capsid core that encloses the viral RNA genome and a small complement of proteins. The final step of this process involves severing the SP1 peptide from the CA-SP1 maturation intermediate, which triggers the condensation of the CA protein into the capsid shell. The details of the overall mechanism, including the conformation of the SP1 peptide in CA-SP1, are still under intense debate. In this report, we examine tubular assemblies of CA and the CA-SP1 maturation intermediate using magic angle spinning (MAS) NMR spectroscopy. At magnetic fields of 19.9 T and above, outstanding quality 2D and 3D MAS NMR spectra were obtained for tubular CA and CA-SP1 assemblies, permitting resonance assignments for subsequent detailed structural characterization. Dipolar- and scalar-based correlation experiments unequivocally indicate that SP1 peptide is in a random coil conformation and mobile in the assembled CA-SP1. Analysis of two CA protein sequence variants reveals that, unexpectedly, the conformations of the SP1 tail, the functionally important CypA loop, and the loop preceding helix 8 are modulated by residue variations at distal sites. These findings provide support for the role of SP1 as a trigger of the disassembly of the immature CA capsid for its subsequent de novo reassembly into mature cores and establish the importance of sequence-dependent conformational plasticity in CA assembly.


Subject(s)
Capsid Proteins/chemistry , Capsid Proteins/metabolism , HIV Infections/virology , HIV-1/chemistry , HIV-1/metabolism , Amino Acid Sequence , Capsid Proteins/ultrastructure , Gene Products, gag/chemistry , Gene Products, gag/metabolism , Gene Products, gag/ultrastructure , HIV-1/ultrastructure , Models, Molecular , Molecular Sequence Data , Nuclear Magnetic Resonance, Biomolecular , Protein Conformation
17.
J Magn Reson ; 235: 58-65, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23969086

ABSTRACT

We report a 1.5-mm NMR probe based on high temperature superconductors operating at 14.1T optimized for (13)C detection. The probe has a total sample volume of about 35 microliters (µL) with an active volume of 20 µL and provides exceptional mass sensitivity for (13)C detection. The probe also has excellent (1)H sensitivity and employs a (2)H lock; (15)N irradiation capability can be added in the future. The coils are cooled to about 20K using a standard Agilent cryogenic refrigeration system, and the sample temperature is regulated near room temperature. The coil design considerations are discussed in detail. This probe is ideal for directly detected (13)C NMR experiments for natural products chemistry and metabolomics applications, for which 35 µL is an optimal sample volume. The outstanding (13)C sensitivity of this probe allowed us to directly determine the (13)C connectivity on 1.1mg of natural abundance histidine using an INADEQUATE experiment. We demonstrated the utility of this probe for (13)C-based metabolomics using a synthetic mixture of common natural abundance metabolites whose concentrations ranged from 1 to 5mM (40-200 nmol).


Subject(s)
Magnetic Resonance Spectroscopy/instrumentation , Amino Acids/chemistry , Carbon Isotopes , Electromagnetic Fields , Electronics , Equipment Design , Histidine/chemistry , Metabolomics/instrumentation , Metabolomics/methods , Signal-To-Noise Ratio , Temperature
19.
J Magn Reson ; 221: 110-6, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22750638

ABSTRACT

A tunable 900 MHz transmit/receive volume coil was constructed for ¹H MR imaging of biological samples in a 21.1 T vertical bore magnet. To accommodate a diverse range of specimen and RF loads at such a high frequency, a sliding-ring adaptation of a low-pass birdcage was implemented through simultaneous alteration of distributed capacitance. To make efficient use of the constrained space inside the vertical bore, a modular probe design was implemented with a bottom-adjustable tuning and matching apparatus. The sliding ring coil displays good homogeneity and sufficient tuning range for different samples of various dimensions representing large span of RF loads. High resolution in vivo and ex vivo images of large rats (up to 350 g), mice and human postmortem tissues were obtained to demonstrate coil functionality and to provide examples of potential applications at 21.1 T.


Subject(s)
Neuroimaging/instrumentation , Algorithms , Alzheimer Disease/pathology , Animals , Brain/pathology , Cadaver , Electromagnetic Fields , Equipment Design , Humans , Mice , Phantoms, Imaging , Rats , Rats, Sprague-Dawley
20.
J Am Chem Soc ; 134(22): 9022-5, 2012 Jun 06.
Article in English | MEDLINE | ID: mdl-22616841

ABSTRACT

As a small tetrameric helical membrane protein, the M2 proton channel structure is highly sensitive to its environment. As a result, structural data from a lipid bilayer environment have proven to be essential for describing the conductance mechanism. While oriented sample solid-state NMR has provided a high-resolution backbone structure in lipid bilayers, quaternary packing of the helices and many of the side-chain conformations have been poorly restrained. Furthermore, the quaternary structural stability has remained a mystery. Here, the isotropic chemical shift data and interhelical cross peaks from magic angle spinning solid-state NMR of a liposomal preparation strongly support the quaternary structure of the transmembrane helical bundle as a dimer-of-dimers structure. The data also explain how the tetrameric stability is enhanced once two charges are absorbed by the His37 tetrad prior to activation of this proton channel. The combination of these two solid-state NMR techniques appears to be a powerful approach for characterizing helical membrane protein structure.


Subject(s)
Nuclear Magnetic Resonance, Biomolecular , Viral Matrix Proteins/chemistry , Models, Molecular , Protein Conformation , Viral Matrix Proteins/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...